{
  "meta": {
    "disclaimer": "Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service.",
    "terms": "https://open.fda.gov/terms/",
    "license": "https://open.fda.gov/license/",
    "last_updated": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Montgomeryville",
      "address_1": "103 A Park Drive",
      "reason_for_recall": "Manufacturer issued a voluntary recall on multiple lots of VY(TM)Flush Heparin Lock Flush Syringes therefore Vygon has subsequently initiated a recall on Vygon branded Heparin Lock Flush Syringes and kits containing the syringes.",
      "address_2": "",
      "product_quantity": "",
      "code_info": "Product Code AMS-9437CP  -- lots 1112059, 1112106, 1202101, 1101505, 1101026, 1103020, 1104130, 1103190, and 1109064.",
      "center_classification_date": "20120613",
      "distribution_pattern": "Nationwide Distribution including AZ, CA, DE, FL, IL, IN, IA, KS, KY, MD, MA, MI, MN, MO, NJ, NY, OH, PA, UT, VA, WA, WV, and WI.",
      "state": "PA",
      "product_description": "Churchill Medical Systems, Inc. VAD ACCESS TRAY Kit    Prefilled syringes included in the kit are used to maintain the patency of indwelling catheter lumens",
      "report_date": "20120620",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Vygon Corporation",
      "recall_number": "Z-1806-2012",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "61945",
      "termination_date": "20130311",
      "more_code_info": "",
      "recall_initiation_date": "20120511",
      "postal_code": "18936-9613",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}